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A case of Foix–Chavany–Marie syndrome due to bilateral corona radiata infarcts
Author(s) -
Rossi Fabiana,
Oliva Mariano,
Straccia Giulia,
Fratta Mario,
Ugga Lorenzo,
Tedeschi Enrico,
Melone Mariarosa Anna Beatrice
Publication year - 2019
Publication title -
neurology and clinical neuroscience
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.125
0ISSN - 2049-4173
DOI - 10.1111/ncn3.12302
Subject(s) - medicine , crying , corona radiata (embryology) , palsy , pseudobulbar palsy , dissociation (chemistry) , anatomy , audiology , surgery , pathology , psychiatry , ovarian follicle , hormone , cumulus oophorus , chemistry , alternative medicine
Foix–Chavany–Marie syndrome ( FCMS ) is a rare type of pseudobulbar palsy characterized by automatic‐voluntary dissociation of movements that depend on V, VII , IX , X, and XII cranial nerves. Most of cases are due to bilateral ischemic lesions of anterior opercula, but the syndrome has also been described after unilateral opercular damage either isolated or associated with contralateral cortico‐nuclear tract involvement. Here, we report the clinical and neuroradiological characteristics of a patient with FCMS due to sequential, bilateral, and symmetrical infarcts of corona radiata, presenting with slurred speech, severe hypophonia, and right central‐type facial palsy that rapidly progressed to inability to speak and swallow. In addition, we observed a sudden onset of neuro‐behavioral changes with psychomotor slowing, aggressive, and oppositive conducts along with emotional lability and involuntary crying. To the best of our knowledge, only one other FCMS case has been previously reported with this peculiar lesional topography.